eudamed_udi Primary ID: D-86820221038883N

Luxor (UDI D-86820221038883N)

Manufactured by LUXOR SAĞLIK ÜRÜNLERİ SAN. VE TİC. A.Ş.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Luxor (Model/Catalog Number: 183) is a medical device manufactured by LUXOR SAĞLIK ÜRÜNLERİ SAN. VE TİC. A.Ş.. This product is indexed under FDA Product Code / Category Classification M03050299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 183
Product Code / EMDN: M03050299
Device Name: Boksör Kırığı Ateli
Database Sync Date: 2026-08-09 16:45:52

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Luxor?

The registered manufacturer of record for Luxor is LUXOR SAĞLIK ÜRÜNLERİ SAN. VE TİC. A.Ş..

What is the Primary UDI-DI identifier for Luxor?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-86820221038883N.

What classification code is assigned to this device?

This device is registered under product classification code M03050299.

Similar Classification Devices (M03050299)

Other Devices by LUXOR SAĞLIK ÜRÜNLERİ SAN. VE TİC. A.Ş.

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